Arginase deficiency masked by cerebral palsy and coagulopathy—Three varied presentations of Latin American origin.

Autor: Mills, Shelby L., Roberts, Paige, Ashfaq, Myla, Leal, Kathryn, Northrup, Hope, Brown, Deborah L., Rodriguez‐Buritica, David, Farach, Laura S.

Publikováno v: Journal of Inherited Metabolic Disease Reports; Nov2023, Vol. 64 Issue 6, p434-439, 6p

Arginase deficiency masked by cerebral palsy and coagulopathy-Three varied presentations of Latin American origin.

Autor: Mills SL; Department of Pediatrics, Division of Medical Genetics McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital Houston Texas USA.; College of Osteopathic Medicine of the Pacific-Northwest Western University of Health Sciences Lebanon Oregon USA., Roberts P; Department of Pediatrics, Division of Medical Genetics McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital Houston Texas USA., Ashfaq M; Department of Pediatrics, Division of Medical Genetics McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital Houston Texas USA., Leal K; Department of Pediatrics, Division of Medical Genetics McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital Houston Texas USA., Northrup H; Department of Pediatrics, Division of Medical Genetics McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital Houston Texas USA., Brown DL; Department of Pediatrics, Division of Hematology Oncology McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital Houston Texas USA., Rodriguez-Buritica D; Department of Pediatrics, Division of Medical Genetics McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital Houston Texas USA., Farach LS; Department of Pediatrics, Division of Medical Genetics McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital Houston Texas USA.

Publikováno v: JIMD reports [JIMD Rep] 2023 Oct 21; Vol. 64 (6), pp. 434-439. Date of Electronic Publication: 2023 Oct 21 (Print Publication: 2023).